Q8WU58 (F222B_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
March 6, 2013.
Version 66.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Protein FAM222B | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 562 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Sequence similarities | Belongs to the FAM222 family. |
| Sequence caution | The sequence BAA90974.1 differs from that shown. Reason: Frameshift at position 433. The sequence BAB15306.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Polymorphism |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 562 | 562 | Protein FAM222B | PRO_0000274245 | |||||
Regions | |||||||||
| Compositional bias | 148 – 220 | 73 | Gln-rich | ||||||
Natural variations | |||||||||
| Natural variant | 471 | 1 | L → S. Corresponds to variant rs2043031 [ dbSNP | Ensembl ]. | VAR_050900 | |||||
| Natural variant | 542 | 1 | G → S. Corresponds to variant rs36029715 [ dbSNP | Ensembl ]. | VAR_050901 | |||||
Experimental info | |||||||||
| Sequence conflict | 15 | 1 | L → P in BAA91757. Ref.1 | ||||||
| Sequence conflict | 261 | 1 | Q → R in BAA91757. Ref.1 | ||||||
| Sequence conflict | 557 | 1 | Q → L in BAA91757. Ref.1 | ||||||
Sequences
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References
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK000147 mRNA. Translation: BAA90974.1. Frameshift. AK001562 mRNA. Translation: BAA91757.1. AK025980 mRNA. Translation: BAB15306.1. Different initiation. AC010761 Genomic DNA. No translation available. AC024267 Genomic DNA. No translation available. BC021228 mRNA. Translation: AAH21228.1. |
| IPI | IPI00291010. |
| RefSeq | NP_001070966.1. NM_001077498.1. NP_060652.2. NM_018182.2. |
| UniGene | Hs.564533. |
3D structure databases | |
| ProteinModelPortal | Q8WU58. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | Q8WU58. 3 interactions. |
PTM databases | |
| PhosphoSite | Q8WU58. |
Polymorphism databases | |
| DMDM | 74730670. |
Proteomic databases | |
| PaxDb | Q8WU58. |
| PRIDE | Q8WU58. |
Protocols and materials databases | |
| DNASU | 55731. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000341217; ENSP00000343115; ENSG00000173065. ENST00000452648; ENSP00000413645; ENSG00000173065. ENST00000581407; ENSP00000462419; ENSG00000173065. |
| GeneID | 55731. |
| KEGG | hsa:55731. |
| UCSC | uc002hct.1. human. |
Organism-specific databases | |
| CTD | 55731. |
| GeneCards | GC17M027086. |
| H-InvDB | HIX0013663. |
| HGNC | HGNC:25563. FAM222B. |
| HPA | HPA051840. |
| neXtProt | NX_Q8WU58. |
| PharmGKB | PA142672246. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG47137. |
| HOGENOM | HOG000111757. |
| HOVERGEN | HBG058998. |
| InParanoid | Q8WU58. |
| OMA | HLQQMCG. |
| OrthoDB | EOG45QHD5. |
Gene expression databases | |
| ArrayExpress | Q8WU58. |
| Bgee | Q8WU58. |
| CleanEx | HS_C17orf63. |
| Genevestigator | Q8WU58. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| ChiTaRS | FAM222B. human. |
| GenomeRNAi | 55731. |
| NextBio | 60652. |
Entry information
| Entry name | F222B_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8WU58 Secondary accession number(s): Q9H6F3, Q9NVJ4, Q9NXN6 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 17 Human chromosome 17: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| SIMILARITY comments Index of protein domains and families |

Clusters with
